免疫球蛋白 A 肾病给美国患者和护理伙伴带来的人文负担。

IF 3.3 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Quality of Life Research Pub Date : 2024-10-26 DOI:10.1007/s11136-024-03813-x
Justyna Szklarzewicz, Ute Floege, Daniel Gallego, Keisha Gibson, Kamyar Kalantar-Zadeh, Kelly Helm, Dale Robinson, Bonnie Schneider, Philip Smith, Kjell Tullus, Ali Poyan-Mehr, Bruce Hendry, Bridget L Balkaran, Adam K Jauregui, Aolin Wang, Ian Nason, Nisha C Hazra, Chunyi Xu, Jingyi Liu, Zheng-Yi Zhou, Mark Bensink
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引用次数: 0

摘要

目的:这项横断面调查研究从身心健康相关生活质量(HRQoL)和工作效率的角度量化了免疫球蛋白A肾病(IgAN)给原发性IgAN成人患者及其护理伙伴带来的人文负担。方法:使用经过验证的工具评估 HRQoL(01/31/22 - 05/31/23),包括 KDQoL-36(与 SF-12)、GAD-7(焦虑)、PHQ-9(抑郁)和 WPAI:SHP(工作效率)。对参与者的特征和总分/领域分进行了总结,并将选定的结果与外部无肾脏病队列进行了比较:研究共纳入了 117 名成人 IgAN 患者及其护理伴侣,以及一名无护理伴侣的成人。患者和护理伙伴的平均年龄分别为 38.0 岁(标清:8.6 岁)和 40.2 岁(11.8 岁);女性分别占 55.9% 和 43.6%。患者的身体和心理 SF-12 平均得分分别为 46.7 分(标度:8.0)和 41.9 分(9.2),护理伙伴的身体和心理 SF-12 平均得分分别为 50.7 分(7.3)和 43.7 分(10.24)。与美国普通人群相比,患者的 SF-12 指标和护理人员的精神指标都明显较差。在患者中,27.1%患有中度/重度焦虑症,49.2%至少患有中度抑郁症。与外部对照组相比,患者的焦虑(6.6 对 5.4)和抑郁(8.1 对 6.6;均为 p)严重程度明显更高:美国成人 IgAN 患者及其护理伙伴的身心健康生活质量受到损害,抑郁和焦虑水平升高,这突出表明需要有效的 IgAN 治疗方法和护理伙伴支持。
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The humanistic burden of immunoglobulin A nephropathy on patients and care-partners in the United States.

Purpose: This cross-sectional survey study quantified the humanistic burden of immunoglobulin A nephropathy (IgAN), in terms of physical and mental health-related quality of life (HRQoL) and work productivity, among adults with primary IgAN and their care-partners.

Methods: HRQoL was assessed (01/31/22 - 05/31/23) with validated tools including the KDQoL-36 (with SF-12), GAD-7 (anxiety), PHQ-9 (depression), and WPAI: SHP (work productivity). Participant characteristics and total/domain scores were summarized; selected outcomes were compared to an external, kidney disease-free cohort.

Results: 117 adults with IgAN and their care-partner pairs, and one adult without a care-partner, were included. The mean ages of patients and care-partners were 38.0 (SD: 8.6) and 40.2 (11.8) years, respectively; 55.9% and 43.6% were female. Mean physical and mental SF-12 scores for patients were 46.7 (SD: 8.0) and 41.9 (9.2), respectively, and 50.7 (7.3) and 43.7 (10.24) for care-partners. Both SF-12 components for patients, and the mental component for care-givers, were significantly worse compared to the US general population. Among patients, 27.1% had moderate/severe anxiety and 49.2% reported at least moderate depression. Compared to external controls, patients experienced significantly higher severity of anxiety (6.6 vs. 5.4) and depression (8.1 vs. 6.6; both p < 0.0001). Among care-partners, 13.7% experienced moderate anxiety and 37.8% experienced moderate/moderately-severe depression. Among employed individuals, both groups reported IgAN-related absenteeism (8.8-9.4%), presenteeism (25.1-25.9%), and overall work impairment (30.4-30.5%).

Conclusion: US adults with IgAN and their care partners experience impairments to mental and physical HRQoL and heightened levels of depression and anxiety, underscoring the need for effective IgAN therapies and care-partner support.

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来源期刊
Quality of Life Research
Quality of Life Research 医学-公共卫生、环境卫生与职业卫生
CiteScore
6.50
自引率
8.60%
发文量
224
审稿时长
3-8 weeks
期刊介绍: Quality of Life Research is an international, multidisciplinary journal devoted to the rapid communication of original research, theoretical articles and methodological reports related to the field of quality of life, in all the health sciences. The journal also offers editorials, literature, book and software reviews, correspondence and abstracts of conferences. Quality of life has become a prominent issue in biometry, philosophy, social science, clinical medicine, health services and outcomes research. The journal''s scope reflects the wide application of quality of life assessment and research in the biological and social sciences. All original work is subject to peer review for originality, scientific quality and relevance to a broad readership. This is an official journal of the International Society of Quality of Life Research.
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